A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878155



Internal ID22653119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23725148..23787394hg38UCSC Ensembl
chrX:23743265..23805511hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3862247
hg1962247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451649
Samples
Known GenesACOT9, SAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878155
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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